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Mojo Bleeder Holster Kit

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
Mojo Bleeder Holster Kit FDA UDI
Generic Name
Wound dressing kit, medicated, non-sterile FDA UDI
Device Name
This kit treats Massive Hemorrhage and comes in nylon holster style belt pouch. The kit contains Celox Rapid hemostatic gauze, and tourniquet of choice and exam gloves. The pouch has a vertical belt loop and can be worn on your standard 2” wide utility and gun belts. FDA UDI
Model / Reference
01 FDA UDI
Description
This kit treats Massive Hemorrhage and comes in nylon holster style belt pouch. The kit contains Celox Rapid hemostatic gauze, and tourniquet of choice and exam gloves. The pouch has a vertical belt loop and can be worn on your standard 2” wide utility and gun belts. FDA UDI

Identifiers

Catalog Number
88-115-03 FDA UDI
Primary DI / UDI-DI
M689881150301 FDA UDI
FDA Product Code
GAX FDA UDI
FRO FDA UDI
GMDN Term
Wound dressing kit, medicated, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5900 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Mojo Bleeder Holster Kit by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9c538485-5993-4ef4-bbe3-d7691fe76d55 35 fields · synced Jun 7, 2026